Searchable abstracts of presentations at key conferences in endocrinology

ea0029p184 | Bone & Osteoporosis | ICEECE2012

The body mass index and heel quantitative ultrasound analyze in 300 women

Carsote M. , Voicu G. , Radoi V. , Ene C. , Poiana C. , Coculescu M.

Introduction: The heel Quantitative Ultrasound (QUS) evaluates the bone health, with good results if the clinical risk factors are also evaluated for each patient. Among these, the body mass index (BMI) may be protective or risk factor for a fragility fracture, depending on the values.Aim: We present a study in postmenpausal women evaluated by QUS and BMI.Patients & method: This is a study in 330 patients (women in menopause wh...

ea0029p922 | Female Reproduction | ICEECE2012

Insulin and androgens but not androgen receptor CAGn polymorphysm are determinant factors for hirsutism severity in PCOS

Baculescu N. , Radian S. , Gussi I. , Aflorei D. , Poiana C. , Grigorescu F. , Coculescu M.

Background: Hirsutism is a major feature of the polycystic ovary syndrome (PCOS) and the only accepted clinical sign of hyperandrogenism for its diagnosis, according to the androgen excess society (AES) recommendations. Previous studies demonstrated that hirsutism can be influenced by factors other than hyperandrogenism per se.Aim: To detect factors influencing hirsutism severity in PCOS.Patients and methods: Hundred and sev...

ea0029p965 | Female Reproduction | ICEECE2012

Sertoli cells ovarian tumor- an ovarian incidentaloma?

Poiana C. , Carsote M. , Trifanescu R. , Ene C. , Neamtu C. , Iosif C. , Terzea D.

Introduction: Infertility investigations include uterine–ovarian ultrasound. The incidental finding of a tumor in a young female might associate a potential severe prognosis in otherwise completely asymptomatic patient.Aim: We present a case of a young female with an accidentally discovered ovarian tumor.Case report: S.M. 35-year female patient is admitted for infertility. Her family and personal medical history is irrelevant....

ea0029p1510 | Pituitary Clinical | ICEECE2012

Follow up of pituitary incidentaloma: a study in 140 patients

Poiana C. , Carsote M. , Trifanescu R. , Danciulescu-Miulescu R. , Musat M. , Hortopan D. , Dumitrascu A.

Introduction: Pituitary incidentaloma is a relatively frequent imagistic finding. Since no therapy is necessary, the follow up protocol is the most important in patients’ approach.Aim: We present a study in patients diagnosed with pituitary incidentaloma, admitted in I.Parhon, Bucharest, between 1999 and 2011.Patients and method: This is a retrospective study in 140 patients, diagnosed with pituitary incidentaloma based on CT ...

ea0026p547 | Bone/calcium/Vitamin D | ECE2011

The QUS fracture risk groups: unifactorial analyze regarding bone markers and DXA assessment

Carsote Mara , Chirita Corina , Radoi Valentin , Ene Cristina , Gruia Adriana , Voicu Gabriela , Poiana Catalina , Coculescu Mihail

Introduction: The quantitative ultrasound (QUS) is an useful tool in the evaluation of the fragility fracture risk.Aim and study design: We performed the QUS fragility fracture risk groups (valided by the golden standard DXA) by a unifactorial analyze including the bone markers.Method: The cut offs used were: SI≤59U (high risk), SI≥83U (low risk), and medium risk with SI between 59 and 83U. The QUS analyze was performed...

ea0026p629 | Clinical case reports | ECE2011

Unexpected association: Turner syndrome and hypopituitarism: a case report

Cucu C , Poiana C , Hortopan D , Dumitrascu A , Popa O , Gurau S , Danciulescu R , Musat M

Introduction: Turner syndrome is a common cause of dwarfism and hypogonadism as is pituitary failure. However the association of the two is rarely thought and reported in the literature. We present two cases of women with hypogonadism diagnosed with Turner syndrome with various degrees of pituitary insuficiency.Case report: The first case presented at 16 years with secondary amenorrhea and showed slightly disharmonic dwarfism. A hypogonadotropic hypogona...

ea0022p56 | Adrenal | ECE2010

Arterial and venous thrombotic events in Cushing's syndrome

Poiana Catalina , Chirita Corina , Carsote Mara , Ene Cristina , Samoila Ramona , Trifanescu Raluca , Gheorghiu Monica , Coculescu Mihail

Background: Cushing’s syndrome (CS) is associated with a hypercoagulable state and an increased risk for acute coronary syndromes, stroke, and deep vein thrombosis (DVT).Aim: To assess the prevalence of thrombotic events in a series of patients with CS.Patients and methods: Notes of 113 patients with CS were retrospectively reviewed.Results: Instable angina was diagnosed in ten women, aged 52.1±12.2...

ea0022p163 | Cardiovascular endocrinology and lipid metabolism | ECE2010

Pitfalls in endocrine assessment of systemic hypertension in young people

Trifanescu Raluca-Alexandra , Poiana Catalina , Caragheorgheopol Andra , Stefanescu Anamaria , Coculescu Mihail

Background: Endocrine hypertension accounts for around 3% of the secondary forms of hypertension and screening of young hypertensive patients for secondary causes is mandatory.Aim: To present difficulties in endocrine assessment of arterial hypertension in people younger than 40 years.Patients and methods: Twenty-two patients (15 M/7 F), aged 27.1±7.7 years (range:16-40 years), with systemic hypertension (systolic blood pressu...

ea0022p247 | Clinical case reports and clinical practice | ECE2010

A tale to tell: how lupus led to Graves' disease

Musat Madalina , Giurca Camelia , Aflorei Daniela , Lupu Anca , Dumitrascu Anda , Milicescu Mihaela , Danciulescu Rucsandra , Poiana Catalina

Introduction: Despite the presence of antinuclear (ANA) and anti DNA antibodies in Graves’ disease, the association with Systemic Lupus Erythematosus (SLE) is rare. Responsible for this association seem to be mutations in the PTPN22 gene.Case Report: We report a case of a 27-year-old woman, who presented in January 2009 in our department, at 6 months postpartum, after extensive investigations for autoimmune disease. She had negative results for poly...

ea0022p455 | Endocrine tumours &amp; neoplasia (<emphasis role="italic">Generously supported by Novartis</emphasis>) | ECE2010

Clinical characteristics of incidentally discovered phaeochromocytomas

Gheorghiu Monica Livia , Baciu Ionela , Mangalagiu Mara , Banaru Ana , Poiana Catalina , Badiu Corin , Coculescu Mihai

Introduction: Phaeochromocytomas (PHEO) are tumours of the chromaffin cells and are usually detected due to the typical symptom triad including headache, palpitations and sweating associated with persistent and/or paroxysmal blood hypertension. An increasing proportion of PHEO is incidentally discovered upon abdominal imaging.Objective: To analyse the clinical characteristics of the incidentally discovered phaeochromocytomas.Method...